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nsv7078062

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:773,567

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1730 SVs from 72 studies. See in: genome view    
    Submitted genomic99,955,191-100,728,757Question Mark
    Overlapping variant regions from other studies: 1730 SVs from 72 studies. See in: genome view    
    Remapped(Score: Perfect):102,717,473-103,491,039Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7078062Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr999,955,191100,728,757
    nsv7078062RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9102,717,473103,491,039

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18785947inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18785947Submitted genomicNC_000009.12:g.999
    55191_100728757inv
    GRCh38 (hg38)NC_000009.12Chr999,955,191100,728,757
    nssv18785947RemappedPerfectNC_000009.11:g.102
    717473_103491039in
    v
    GRCh37.p13First PassNC_000009.11Chr9102,717,473103,491,039

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv187859471.4e-054274600
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